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. 2008 Dec;180(4):2033–2055. doi: 10.1534/genetics.108.095042

TABLE 4.

Sumoylation mutants do not display synthetic lethality with either KAR9 or dynein pathway mutants

Cross Viability Tetrad (PD:TT:NPD) Double mutant (viable/predicted)
cst9Δ × jnm1Δ Viable 25 (3:16:6) 27/28
siz1Δ × jnm1Δ Viable 24 (3:19:2) 22/23
cst9Δ × dhc1Δ Viable 27 (3:20:4) 28/28
siz1Δ × dhc1Δ Viable 22 (4:14:4) 22/22
nfi1Δ × dhc1Δ Viable 27 (2:21:4) 28/29
SMT3 × jnm1Δ Viable 27 (8:15:4) 20/23
smt3-11 × jnm1Δ Viable 28 (6:16:6) 28/28
smt3-12 × jnm1Δ Viable 16 (2:12:2) 16/16
cst9Δ × kar9Δ Viable 31 (7:18:6) 28/30
siz1Δ × kar9Δ Viable 28 (2:21:5) 30/31
nfi1Δ × kar9Δ Viable 30 (9:19:2) 23/23
SMT3 × kar9Δ Viable 33 (5:25:3) 30/31
smt3-11 × kar9Δ Viable 19 (1:14:4) 20/22
smt3-12 × kar9Δ Viable 20 (3:11:6) 23/23

Double mutants between sumoylation mutants and KAR9 or dynein pathway mutants were generated by meiotic crosses and scored for growth after 2–3 days. The tetrads were incubated at 30° except SMT3, smt3-11, and smt3-12 crosses, which were grown at 23°. The double mutant, single mutant, and wild type exhibited no difference in growth at 30° or 23°. Thus the double mutants were scored as viable. The following parental strains were used in the crosses: cst9Δ (yRM7166), siz1Δ (yRM7140), nfi1Δ/siz2Δ (yRM7248), SMT3 (yRM6491), smt3-11 (yRM6493), smt3-12 (yRM6492), jnm1Δ (yRM6727), dhc1Δ (yRM373), and kar9Δ (yRM1340).